The presence of a translocation 21/13-15 is related in 46 chromosomes, karyotypes of a mongoloid male child (Down's syndrome). The abnormal chromosome was transmitted by the mother of the patient. The possible deficiency of translocated chromosome 21 and the possible origin of the anomaly in the family was discussed and the presence of a markedly large Y chromosome in the karyotypes of the patient as in those of his father was also noted
A Research Report submitted to the Faculty of Medicine, University of the Witwatersrand, Johannesbur...
Parental mosaicism for trisomy-21 is a recognized reason for the birth of mongol children, and the p...
A 3 month-old boy with a karyotype of 48, XYY, + 21 is reported. The patient had the typical feature...
The presence of a translocation 21/13-15 is related in 46 chromosomes, karyotypes of a mongoloid mal...
We report a case of Down syndrome with unusual chromosome translocation. The proband is a 1 year old...
Among 17786 karyotyres performed in our center,during 18 years (1357-1375),1300(7.3%) cases of chrom...
The presence of a translocation between two chromosomes in the I3-I5 (D) group does not usually give...
Cytogenetic analysis in 60 clinically suspected cases of Down syndrome and their parents was carrie...
We describe a 17-month-old infant with clinical features of Down syndrome and a normal karyotype by ...
Background – Down syndrome is the most common cause of mental retardation observed in approximately ...
The origin of meiotic nondisjunction of the extra chromosomes X and 21 was studied in a patient with...
ABSTRACT Double aneuploidy involving XYY and trisomy 21 is rare. XYY/XY mosaicism has been described...
PubMedID: 18990986Reciprocal translocation carriers have reduced fertility, increased risk of sponta...
SUMMARY A retrospective cytogenetic study was carried out on the parents of children with regular tr...
Chromosome abnormalities in structure as well as number have often been found to be associated with ...
A Research Report submitted to the Faculty of Medicine, University of the Witwatersrand, Johannesbur...
Parental mosaicism for trisomy-21 is a recognized reason for the birth of mongol children, and the p...
A 3 month-old boy with a karyotype of 48, XYY, + 21 is reported. The patient had the typical feature...
The presence of a translocation 21/13-15 is related in 46 chromosomes, karyotypes of a mongoloid mal...
We report a case of Down syndrome with unusual chromosome translocation. The proband is a 1 year old...
Among 17786 karyotyres performed in our center,during 18 years (1357-1375),1300(7.3%) cases of chrom...
The presence of a translocation between two chromosomes in the I3-I5 (D) group does not usually give...
Cytogenetic analysis in 60 clinically suspected cases of Down syndrome and their parents was carrie...
We describe a 17-month-old infant with clinical features of Down syndrome and a normal karyotype by ...
Background – Down syndrome is the most common cause of mental retardation observed in approximately ...
The origin of meiotic nondisjunction of the extra chromosomes X and 21 was studied in a patient with...
ABSTRACT Double aneuploidy involving XYY and trisomy 21 is rare. XYY/XY mosaicism has been described...
PubMedID: 18990986Reciprocal translocation carriers have reduced fertility, increased risk of sponta...
SUMMARY A retrospective cytogenetic study was carried out on the parents of children with regular tr...
Chromosome abnormalities in structure as well as number have often been found to be associated with ...
A Research Report submitted to the Faculty of Medicine, University of the Witwatersrand, Johannesbur...
Parental mosaicism for trisomy-21 is a recognized reason for the birth of mongol children, and the p...
A 3 month-old boy with a karyotype of 48, XYY, + 21 is reported. The patient had the typical feature...